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2-丙酰基-3,4,5,6-四氢 | 80933-75-1

中文名称
2-丙酰基-3,4,5,6-四氢
中文别名
——
英文名称
1-(3,4,5,6-tetrahydro-2-pyridyl)-1-propanone
英文别名
2-Propionyl-3,4,5,6-tetrahydropyridine;1-(2,3,4,5-tetrahydropyridin-6-yl)propan-1-one
2-丙酰基-3,4,5,6-四氢化学式
CAS
80933-75-1
化学式
C8H13NO
mdl
——
分子量
139.197
InChiKey
GGYSXLMPBBMRHY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    224.0±23.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)
  • 保留指数:
    1148

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    29.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-丙酰基吡啶 在 Rh/Al2O3 Celite 、 氢气 、 silver carbonate 作用下, 以 乙醇 为溶剂, 反应 59.0h, 生成 2-丙酰基-3,4,5,6-四氢
    参考文献:
    名称:
    Volatile Constituents of Semnostachya menglaensis Tsui
    摘要:
    Semnostachya menglaensis Tsui (Acanthaceae) is a rare plant indigenous to Mengla in the tropical rainforest of the Xishuangbanna prefecture in the south of Yunnan province, People's Republic of China. When the leaves are crushed, a characteristic smell of basmati rice or pandan leaves develops. Their hexane extract, prepared from a specimen growing in a greenhouse of the botanical garden of the Kunming Institute of Botany, contains 1-(3,4,5,6-tetrahydro-2-pyridyl)-1-propanone (41.2%) and 1-(1,4,5,6-tetrahydro-2-pyridyl)-1-propanone (37.5%) which constitute the main part of the volatile compounds. Minor components are 1-(3,4,5,6-tetrahydro-2-pyridyl)-1-ethanone (4.9%), 1-(1,4,5,6-tetrahydro-2-pyridyl)-1-ethanone (4.8%), 1-(2-piperidyl)-1-propanone (5.2%), 1-octen-3-ol (3.2%), 1-octen-3-one (1.9%), and 3-octanol and 1-(2-pyridyl)-1-propanone in trace amounts.
    DOI:
    10.1021/jf051632d
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文献信息

  • METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED
    申请人:Morere Alain
    公开号:US20120100274A1
    公开(公告)日:2012-04-26
    The present invention relates to a method for synthetizing a compound of the following formula (I): wherein R is a methyl or ethyl group, n is 1 or 2, and X is a CH 2 or CD 2 group, from a compound of the following formula (II): wherein R and n are as defined above, and also relates to a method for assaying the compounds of the formula (I) using a corresponding deuterated derivative as an internal reference, as well as to the use of ketal derivatives of compounds of the formula (I) as a stable precursor, in particular in a flavoring composition.
    本发明涉及一种从以下式(I)的化合物合成方法:其中R为甲基或乙基基团,n为1或2,X为CH2或CD2基团,从以下式(II)的化合物开始:其中R和n如上所定义,并且涉及一种使用相应的氘代衍生物作为内部参考的方法来测定式(I)的化合物,以及将式(I)的化合物的缩酮衍生物用作稳定前体的用途,特别是在调味组合物中。
  • Flavor Contribution and Formation of the Intense Roast-Smelling Odorants 2-Propionyl-1-pyrroline and 2-Propionyltetrahydropyridine in Maillard-Type Reactions
    作者:Thomas Hofmann、Peter Schieberle
    DOI:10.1021/jf971101s
    日期:1998.7.1
    Application of aroma extract dilution analysis on two different model mixtures of proline and glucose, reacted under aqueous or dry-heating conditions, revealed 2-propionyl-1-pyrroline (PP) and 2-propionyltetrahydropyridine (PTHP; occurring in two tautomers), besides 2-acetyl-1-pyrroline and 2-acetyltetrahydropyridine, as important roast-smelling odorants in both mixtures. A comparison of the isotope distribution in PP and PTHP formed from either C-13(6)-labeled or unlabeled glucose suggested a formation pathway for both odorants from the same intermediate, l-pyrroline, when reacted with either 2-oxobutanal (yielding PP) or 1-hydroxy-2-butanone (yielding PTHP). 2-Oxobutanal, a possible precursor of 1-hydroxy-2-butanone, was shown to be formed in high yields (29 mol %) by reacting acetaldehyde and glycolaldehyde, two well-known degradation products of carbohydrates.
  • Novel Syntheses of the Major Flavor Components of Bread and Cooked Rice
    作者:Norbert De Kimpe、Marian Keppens
    DOI:10.1021/jf950728c
    日期:1996.1.1
    A new synthetic pathway toward the Maillard flavor compounds 6-acyl-1,2,3,4-tetrahydropyridines and 2-acetyl-1-pyrroline is presented. The reaction sequence involves deprotonation of a vicinal diimine and subsequent alkylation with an N,N-diprotected omega-bromoalkylamine, followed by deprotection and intramolecular transimination of the functionalized intermediate. Acidic workup affords the above-mentioned heterocycles, which are principal flavor constituents of bread and cooked rice, respectively. In addition, the synthesis of the more stable diethyl acetal of 2-acetyl-1-pyrroline is described.
  • METHODE DE SYNTHESE DE LA 2-ACETYL-1-PYRROLINE ET DE SON PRECURSEUR STABLE, MARQUE ISOTOPIQUEMENT OU NON
    申请人:Centre National de la Recherche Scientifique (C.N.R.S.)
    公开号:EP2445874B1
    公开(公告)日:2017-11-29
  • METHODE DE SYNTHESE DE LA 2 -ACETYL-1-PYRROLINE ET DE SON PRECURSEUR STABLE, MARQUE ISOTOPIQUEMENT OU NON
    申请人:Centre National de la Recherche Scientifique CNRS
    公开号:EP2445874A1
    公开(公告)日:2012-05-02
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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